Hydrochloric Acid → 1-(Imidazo[1,2-a]pyridin-6-yl)propan-2-one

HRID 414322

Reaktionsgleichung

Reaktionsgleichung von HRID 414322
[N+]([C:4]([CH3:15])=[CH:5][C:6]1[CH:7]=[CH:8][C:9]2[N:10]([CH:12]=[CH:13][N:14]=2)[CH:11]=1)([O-])=O.Cl.[OH2:17]>CCO>[N:14]1[CH:13]=[CH:12][N:10]2[CH:11]=[C:6]([CH2:5][C:4](=[O:17])[CH3:15])[CH:7]=[CH:8][C:9]=12

Komponenten

5

Edukt 3

HCID 313Hydrochloric AcidHCID 962WaterHCID 539155686-(2-Nitro-1-propenyl)imidazo[1,2-a]pyridine

Produkt 1

HCID 138523111-(Imidazo[1,2-a]pyridin-6-yl)propan-2-one

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 702EthanolLösungsmittel

Versuchsvorschrift

In 25 ml of water and 25 ml of EtOH, 1.14 g of 6-(2-nitro-1-propenyl)imidazo[1,2-a]pyridine was heated to 80° C. together with 100 mg of ferrous chloride. With stirring, 2.5 ml of conc. hydrochloric acid was added at a refluxing rate and the mixture was stirred for 1 hour. Upon heating, insoluble matter was removed by filtration. After the insoluble matter was thoroughly washed with ethanol, the solvent was removed by distillation under reduced pressure. An aqueous sodium bicarbonate solution was added to the residue and the mixture was extracted with chloroform. After washing with water and drying over magnesium sulfate, chloroform was removed by distillation under reduced pressure. The residue was purified by column chromatography to obtain 500 mg of 1-(imidazo[1,2-a]pyridin-6-yl)-2-propanone.

Aufarbeitung

  1. stirringthe mixture was stirred for 1 hour
  2. temperatureUpon heating
  3. custominsoluble matter was removed by filtration
  4. washAfter the insoluble matter was thoroughly washed with ethanol
  5. customthe solvent was removed by distillation under reduced pressure
  6. additionAn aqueous sodium bicarbonate solution was added to the residue
  7. extractionthe mixture was extracted with chloroform
  8. washAfter washing with water
  9. dry with materialdrying over magnesium sulfate, chloroform
  10. customwas removed by distillation under reduced pressure
  11. customThe residue was purified by column chromatography

Quellen und Nachweise

ORD-Eintrag
ord-36f5757ec41e4f45beb82fbff807494f
Quelldatensatz
uspto-grants-1988_12
Patentnummer
US04791202

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